Differentiation-inducing factor-1は骨髄由来間葉系幹細胞の脂肪細胞分化を促進し、骨芽細胞分化を抑制する

Mesenchymal stem cells (MSCs) are an attractive cell source for tissue regeneration and repair. However, their low differentiation efficacy currently impedes the development of MSC therapy. In this study, we investigated the effects of differentiation-inducing factor-1 (DIF-1) on the differentiation...

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Published in日本薬理学会年会要旨集 p. 1-O-G3-2
Main Authors 豊平, 由美子, 瀧口, 知浩, 松永, 洋明, 石兼, 真, 岸上, 赳大, 幾島, 栄悟, 高橋, 富美
Format Journal Article
LanguageJapanese
Published 公益社団法人 日本薬理学会 2021
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ISSN2435-4953
DOI10.1254/jpssuppl.94.0_1-O-G3-2

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Summary:Mesenchymal stem cells (MSCs) are an attractive cell source for tissue regeneration and repair. However, their low differentiation efficacy currently impedes the development of MSC therapy. In this study, we investigated the effects of differentiation-inducing factor-1 (DIF-1) on the differentiation efficacy of bone marrow-derived MSCs (BM-MSCs) into adipogenic or osteogenic lineages. BM-MSCs were obtained from Sprague-Dawley rats. DIF-1 alone neither affected cell surface antigen expression nor induced adipogenic or osteogenic differentiation. However, DIF-1 significantly enhanced the effects of adipogenic differentiation stimuli, which were evaluated as the number of oil red-O positive cells and the expression of adipocyte differentiation markers. In contrast, DIF-1 significantly attenuated the effects of osteogenic differentiation stimuli, which were evaluated as alizarin red-S positive calcium deposition, and the expression of osteoblast differentiation markers. We further investigated the mechanism by which DIF-1 affects MSC differentiation efficacy and found that glycogen synthase kinase-3 was the main factor mediating the action of DIF-1 on the adipogenic differentiation of BM-MSCs, whereas it was only partially involved in osteogenic differentiation. These results suggest that DIF-1 supports MSC differentiation toward the desired cell fate by enhancing the differentiation efficacy.
Bibliography:94_1-O-G3-2
ISSN:2435-4953
DOI:10.1254/jpssuppl.94.0_1-O-G3-2